STRATA II Adjusment Kit - Indonesia BPOM Medical Device Registration
STRATA II Adjusment Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003125133. The device is manufactured by PMC, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PMC, LLCCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Aug 21, 2021
Expiry Date
Jan 13, 2026
Product Type
Therapeutic Neurology Equipment
Central nervous system fluid shunt and components.
Non Electromedic Non Sterile
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